Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | HCID 54158792 | HCID 54158792 | — |
| Product | HCID 54382601 | HCID 54382601 | — |
Reaction Steps
N-(4-Chlorophenyl)alanine ethyl ester (4.5 g, 0.02 mol), n-butyl iodide (3.6 g, 0.02 mol) and 2,6-lutidine (2.5 g, 0.025 mol) were sealed in a glass tube and the contents were heated at 135° C. for 48 h. The tube was then cooled, and the contents were partitioned between 250 mL ethyl acetate and 200 mL brine. The organic layer was separated, dried over anhyd. sodium sulfate, and concentrated at reduced pressure. The resulting oil was chromatographed on silica gel using heptane:THF (4:1) as the eluant. The ester was isolated as a colorless oil (2.5 g, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747236 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-8811b95d01a945618ba291218b48357b |
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| Source note | uspto-grants-1998_05 |
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